"51660-209-69" National Drug Code (NDC)

Loratadine 1 BLISTER PACK in 1 CARTON (51660-209-69) > 10 TABLET in 1 BLISTER PACK
(Ohm Laboratories Inc.)

NDC Code51660-209-69
Package Description1 BLISTER PACK in 1 CARTON (51660-209-69) > 10 TABLET in 1 BLISTER PACK
Product NDC51660-209
Product Type NameHUMAN OTC DRUG
Proprietary NameLoratadine
Non-Proprietary NameLoratadine
Dosage FormTABLET
UsageORAL
Start Marketing Date20090623
Marketing Category NameANDA
Application NumberANDA076134
ManufacturerOhm Laboratories Inc.
Substance NameLORATADINE
Strength10
Strength Unitmg/1

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